Phenotype #0000128911
| Individual ID |
00163792 |
| Associated disease |
CPDX2 |
| Phenotype details |
several fetal form |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
CPDX-2 |
| Age/Examination |
- |
| Age/Diagnosis |
00y01m |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Fabienne Dufernez |
| Database submission license |
No license selected |
| Created by |
Fabienne Dufernez |
| Date created |
2018-04-12 15:52:39 +02:00 (CEST) |
| Date last edited |
N/A |
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